Thermal Expansion Properties - Solid State Physics - Lecture Slides, Slides of Solid State Physics

This course deals with crystalline solids and is intended to provide students with basic physical concepts and mathematical tools used to describe solids. Key words in this lecture are: Thermal Expansion Properties, Coefficient of Thermal Expansion, Bond Lenght, Bond Energy, Elastic Properties, Atomic Positions and Vibraitons, Thermal Expansions, Heat Capacity, Thermal Conductivity, Thermoelectric Cooling and Heating

Typology: Slides

2012/2013

Uploaded on 12/31/2013

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Scientists do stupid looking things sometimes (though not too
unsafe if they made the material carefully enough)
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Scientists do stupid looking things sometimes (though not too

unsafe if they made the material carefully enough)

- Materials change size when heating.

L^

final

L

initial

L^

initial

(T

final

T

initial

CTE: coefficient ofthermal expansion (units: 1/K)

Tinit Tfinal

Linit Lfinal

THERMAL EXPANSION

  • Melting Temperature, T

m r

smaller Tmlarger Tm

Energy (r)

r^ o

T

m^

is larger if E

o^

is larger.

PROPERTIES FROM BONDING: T

M

  • Elastic modulus, E• E ~ curvature at r

o

crosssectionalarea Ao

 L

length, Lo

F

undeformed

deformed

 L

F A

= E o

Lo Elastic modulus

r

larger Elastic Modulus

smaller Elastic Modulus

Energy

unstretched lengthr^ o

E is larger if curvature is larger.

PROPERTIES FROM BONDING:

Elastic Properties

E similar to spring constant

T^0

T T 2 3

Atomic positions and vibrations

-^

The minimum in an atomic energyvs. interatomic distance curveyields the

near neighbor distance

(bond length).

-^

The width of the curve is proportional to the amplitude ofthermal vibrations for an atom

.

-^

If the curve is symmetric, there isno shift in the average position ofthe atom (the center of the thermalvibrations at any given T).

-^

The coefficient of thermalexpansion is negligible forsymmetric energy wells.

Thermal Expansion

•^

If the curve is not symmetric, the average position in whichthe atom sits shifts with temperature.

-^

Bond lengths therefore change (usually get bigger forincreased T).

-^

Thermal expansion coefficient is nonzero.

Bond energy

Bond length (r)

increasing T

T

r(T5)

r(T1)

T

bond energy vs bond lengthcurve is ā€œasymmetricā€

Thermal expansion example

•^

Example

-^

An Al wire is 10 m long and is cooled from 38 to -1 degreeCelsius. How much change in length will it experience?



l = l

o



l

T

= (10 m) 23.6 x 10

^6

(ļ‚°

C)

^1

ļ‚°C



38

ļ‚°C)

-9.2 mm

Small/Negative thermal expansion

•^

Invar (Ni-Fe alloy) is the most common low thermal expmaterial:

α

/ degree

•^

Some materials have

α

<0 in one dimension and >0 in others.

•^

It is possible, though not intuitive, for materials to have anegative thermal expansion in all dimensions.– An increase in temperature causes the crystal to shrink.

-^

ZrW

O 2

: contracts continuously and linearly from 2 to 1050K 8

-^

Composites could allow zero thermal expansion components (superb foroptics, engine parts, etc).

http://www.dur.ac.uk/john.evans/webpages/research_nteintro.html

HEAT CAPACITY

K

J/mol(

(^

e

temperatur

d

energy

d

dQdT

C

Capacity at constant volume =

C

V

Capacity at constant pressure =

C

P

C

P^

is typically >

C

, but the difference is small for solids. V

When heated, materials experience an increase in T. Thismeans that heat is absorbed.Heat capacity represents the amount of energy required toproduce a unit temperature rise.

2

4.18 J raises 1g of H O by 1 K4.18 J raises 1g of Cu by 11 K

H

O has a higher heat capacity 2

HEAT CAPACITY – The Dulong-Petit Law

N

k 0

b

V^

o^

B

C

of

N k

 D

=Temperature at which

 D

(Cu)

 D

(Al)

 D

(Pb)

T2 > T

T

x

x

heat flux

THERMAL CONDUCTIVITY

^

^

2

nd

2

'^
L
T^
T^
T^
T

k^

if K

f^

T

k^

Fick s

aw

t^

x^

x^

t^

x ^

ļ‚¶^
ļ‚¶^
ļ‚¶^
ļ‚¶^
^
^
^
^
^
^
ļ‚¶^
ļ‚¶^
ļ‚¶^
ļ‚¶^
^
^
^

Fick’s Second Law

- Non-Steady State:

dT/dt is not constant.

- Polymers

PolypropylenePolyethylenePolystyreneTeflon

0.120.46-0.500.130.

k (W/m-K)

- Ceramics

Magnesia (MgO)Alumina (Al2O3)Soda-lime glassSilica (cryst. SiO2)

3839 1.71.

- Metals

AluminumSteelTungstenGold

24752178315

increasing k

Energy TransferBy vibration ofatoms andmotion ofelectronsBy vibration ofatoms By vibration/rotation of chainmolecules

Material

Selected values from Table 19.1,

Callister 6e.

K=k

+kl

:^ e

Again think about band gaps: metals have lots of free electrons(k

is large), while ceramics have few (only ke^

is active).l^

THERMAL CONDUCTIVITY

•^

Thermal conductivity istemperature dependent.– Analagous to electron

scattering.

  • Usually first decreases with

increasing temperature•

Higher Temp=more scatteringof electrons AND phonons,thus less transfer of heat.

  • Then increases at still higher

temperatures due to otherprocesses we havenā€˜tconsidered in this class(radiative heat transfer—eg. IRlamps).

THERMAL CONDUCTIVITY

Thermal conductivity optimization

To maximize thermal conductivity, there are several options:

  • Provide as many free electrons (in the conduction band) as possible -^

free electrons conduct heat more efficiently than phonons.

  • Make crystalline instead of amorphous -^

irregular atomic positions in amorphous materials scatter phonons anddiminish thermal conductivity

  • Remove grain boundaries -^

gb’s scatter electrons and phonons that carry heat

  • Remove pores (air is a terrible conductor of heat)